Canonical Allele Identifier: CA513365578

Gene: TXNRD2

Linked Data

• MyVariant Identifiers: chr22:g.19883093G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19895570G>C , CM000684.2:g.19895570G>C	GRCh38
NC_000022.10:g.19883093G>C , CM000684.1:g.19883093G>C	GRCh37
NC_000022.9:g.18263093G>C	NCBI36
NG_011835.1:g.51267C>G , LRG_417:g.51267C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400521.7:c.786C>G MANE Select	ENSP00000383365.1:p.Ser262=
ENST00000334363.14:c.786C>G	ENSP00000334451.9:p.Ser262=
ENST00000400518.5:c.696C>G	ENSP00000383362.1:p.Ser232=
ENST00000400519.6:c.783C>G	ENSP00000383363.1:p.Ser261=
ENST00000400521.6:c.786C>G	ENSP00000383365.1:p.Ser262=
ENST00000400525.6:c.717C>G	ENSP00000383369.3:p.Ser239=
ENST00000474308.5:c.729C>G	ENSP00000485665.1:p.Ser243=
ENST00000475995.3:c.283C>G
ENST00000491939.6:c.690C>G	ENSP00000485543.1:p.Ser230=
ENST00000494454.5:n.860C>G
ENST00000542719.6:c.498C>G	ENSP00000485128.2:p.Ser166=
ENST00000634537.1:c.15C>G	ENSP00000489208.1:p.Ser5=
ENST00000635155.1:n.372C>G
NM_001282512.1:c.786C>G	NP_001269441.1:p.Ser262=
NM_006440.4:c.786C>G	NP_006431.2:p.Ser262=
NM_001282512.2:c.786C>G	NP_001269441.1:p.Ser262=
NM_001352300.1:c.783C>G	NP_001339229.1:p.Ser261=
NM_001352301.1:c.696C>G	NP_001339230.1:p.Ser232=
NM_001352302.1:c.498C>G	NP_001339231.1:p.Ser166=
NM_001352303.1:c.690C>G	NP_001339232.1:p.Ser230=
NR_147957.1:n.918C>G
NM_006440.5:c.786C>G MANE Select	NP_006431.2:p.Ser262=
NM_001282512.3:c.786C>G	NP_001269441.1:p.Ser262=
NM_001352300.2:c.783C>G	NP_001339229.1:p.Ser261=
NR_147957.2:n.744C>G
NM_001352301.2:c.696C>G	NP_001339230.1:p.Ser232=
NM_001352302.2:c.498C>G	NP_001339231.1:p.Ser166=
NM_001352303.2:c.690C>G	NP_001339232.1:p.Ser230=